23-gauge soft tipped cannulas 1272.SD23

GUDID 18717872002856

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use Epiretinal/inner limiting membrane scraper, single-use
Primary Device ID18717872002856
NIH Device Record Key0629a774-d1a0-4d6e-87b3-66a9b9255a10
Commercial Distribution StatusIn Commercial Distribution
Brand Name23-gauge soft tipped cannulas
Version Model Number1272.SD23
Catalog Number1272.SD23
Company DUNS407522184
Company NameD.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Device Count5
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS108717872002859 [Primary]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]
GS118717872002856 [Unit of Use]

FDA Product Code

HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic
HMXCannula, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-22
Device Publish Date2021-02-01

On-Brand Devices [23-gauge soft tipped cannulas]

187178720028631272.SD23
187178720028561272.SD23

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